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Infusion Pumps

🏥 Medical Devices 4,350 recalls

One lot of SMARTSET GHV Gentamicin Bone Cement is partially agglomerated . This may result in surgical delays while a replacement package of cement is retrieved and mixed.

Feb 11, 2015 Infusion Pumps Nationwide View Details →

Incorrect CT to ED when using the Monaco Image Statistics Tool.

Dec 19, 2014 Infusion Pumps Nationwide View Details →

One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may fail to sound at all volume levels.

Jul 2, 2014 Infusion Pumps Nationwide View Details →

Current labeling indicates that cycling improves device longevity in every programming scenario. However, enabling cycling at certain parameter settings may decrease the device battery longevity. With cycling enabled, longevity estimate displayed on the Model 8840Programmer may be inaccurate.

Jan 9, 2015 Infusion Pumps Nationwide View Details →

One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may fail to sound at all volume levels.

Jul 2, 2014 Infusion Pumps Nationwide View Details →

One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may fail to sound at all volume levels.

Jul 2, 2014 Infusion Pumps Nationwide View Details →

One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may fail to sound at all volume levels.

Jul 2, 2014 Infusion Pumps Nationwide View Details →

One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may fail to sound at all volume levels.

Jul 2, 2014 Infusion Pumps Nationwide View Details →

Ferrule Cap was not removed on some fiber-optic Sensation and Sensation Plus IABC demonstration units. If fiber-optic connector is inserted into the Maquet CS300 or CARDIOSAVE IABP, cap will prevent connection of unit and may become dislodged and remain in IABPs fiber-optic receptacle.

Dec 16, 2014 Infusion Pumps View Details →

The labelling of units from the affected lot indicates that it contains a size 5 LMA Supreme (New Cuff), but may contain a size 4 LMA Supreme (New Cuff).

Jan 13, 2015 Infusion Pumps Nationwide View Details →

Software anomaly related to RECIST1.1 target lesion evaluation criteria in Findings Workflow Module within the Aquarius iNtuition Client Viewer.

Jan 21, 2015 Infusion Pumps Nationwide View Details →

Software error occurs when using remote monitoring; if the remote user tries to stop the free run waveform group, the system will display a message informing the user that they do not have sufficient privilege.

Jan 2, 2015 Infusion Pumps Nationwide View Details →

A manufacturing error resulted in the risk of incorrect proximal and distal balloon inflation port identification on the units. Units have been identified to have the distal balloon inflation port incorrectly labeled as proximal, and, the proximal balloon port incorrectly labeled as distal.

Dec 10, 2014 Infusion Pumps Nationwide View Details →